Not exact matches
Immunotherapy differs from more traditional cancer treatments, such as surgery (cutting malignant
cells out of the body), chemotherapy and radiation (poisoning the deadly mutants), and even the newer, more precise molecular drugs that attempt to jam the
protein signals that tell tumor
cells to keep dividing and conquering.
The cancerous
cells win
out over the healthy blood
cells in the bone marrow, which in turn leads to kidney problems when the cancer
cells make abnormal
proteins instead
of antibodies.
For example, instead
of using the
protein scissors to cut a virus, they can be used to cut
out DNA in a human
cell and replace it with DNA
of the scientist's choosing.
DNA / RNA and
proteins are by far the most important components
of a living organism, carrying
out virtually every function in a
cell.
DNA never leaves the nucleus
of the
cell; its molecular recipes are read
out in the form
of messenger RNA, which leaves the nucleus and enters the cytoplasm, where
proteins are made.
Infectious organisms trip specialized immune
cells in the body and cause them to pump
out proteins called cytokines, which produce inflammation and other hallmarks
of infection, such as chills and fever.
The production
of this
protein in a nerve
cell eventually kills it but it has long been thought that this
protein can not spread
out of the
cell and infect and kill neighbouring ones.
An animal's immune system detects foreign
cells by scanning for
proteins, called antigens, that stick
out from the surface
of each
cell.
But even though IDPs in multicelled organisms make up 30 to 50 percent — depending on the organism —
of the
proteins that genes are able to make, it turns
out that at any given moment, they exist in the
cell in only tiny amounts.
Pediatric immunologists Gurjit Khurana Hershey and Talal Chatila
of the Washington University School
of Medicine in St. Louis and their colleagues set
out to examine the receptor
protein that IL - 4 binds to on white blood
cells.
Studying the rodents more carefully, the researchers determined that Clostridia were having a surprising effect on the mouse gut: Acting through certain immune
cells, the bacteria helped keep peanut
proteins that can cause allergic reactions
out of the bloodstream.
RNA, widely known as a cellular messenger that makes
proteins and carries
out DNA's instructions to other parts
of the
cell, is now understood to perform sophisticated chemical reactions and is believed to perform an extraordinary number
of other functions, at least some
of which are unknown.
But in the 1 September issue
of the Journal
of Clinical Investigation, cardiologist Michael Parmacek and his colleagues at the University
of Chicago describe how they deleted two genes from the common cold virus to make it unable to cause any sniffling or fever, then replaced them with a marker gene that turns
out an easily detected
protein and the SM22 promoter, which turns on expression
of genes in smooth muscle
cells that surround arteries.
In August 1995 they announced that breast milk kills cancer
cells and pinpointed the killer, which turned
out to be one
of the most abundant
proteins in the milk.
In the new work, neurologist Teresa Coelho
of the Hospital de Santo Antonio in Portugal and colleagues tested RNAi in patients who had transthyretin amyloidosis, a fatal genetic disease in which liver
cells pump
out excess amounts
of a
protein called transthyretin.
In all, scientists estimate that the human body contains about 100,000 different
proteins, each the result
of millions
of years
of evolutionary shuffling, culminating in a precise lineup
of pleats, coils, and furrows required to carry
out a specific job in the
cell.
Changes to the properties
of the lipid bilayer component
of the
cell membrane can alter the function
of proteins embedded in the membrane —
proteins that regulate critical functions such as transport
of materials in and
out of the
cell and communication with other
cells.
When they find an intruder, the dendritic
cells brandish a sample (think
of a most - wanted poster) and rush to the lymphatic system, where they present it to T
cells, whose role is to form a posse and fan
out through the body to hunt down and kill any
proteins that look like the poster.
The specialized immune - system function
of dendritic
cells is to sample
proteins and serve as a sort
of security guard, sorting
out alien
proteins from the home team.
This small
protein molecule contains a loop which fits, like a key in a lock, into the ion channel
proteins found on nerve
cell membranes, which are used to transport sodium and potassium ions in and
out of the
cell.
When that
protein is added to the receptor, the receptor gets taken
out of its nanodomain and becomes caught up in the actin filaments that form the
cell's cytoskeleton.
By measuring changes in the levels
of proteins that control each
cell death program and by observing the
cells» physical changes, the team saw clearly that cocaine causes neuronal
cell death through
out -
of - control autophagy.
June's team also wants to knock
out two gene segments that encode different portions
of the
protein that makes up a T
cell's primary receptor so that the engineered NS - ESO - 1 receptor will be more effective.
They might also come up with a way to select the right
cells out of a mixed population; Anand Swaroop, an ophthalmology researcher at the University
of Michigan at Ann Arbor, is working on a way to identify and weed
out the photoreceptor
cells by focusing on
proteins present on
cell surfaces.
RNA messages are copies
of small snippets
of DNA that move
out of the
cell nucleus to be converted into
proteins.
When the
protein is present, these
cells that start
out round and stuck together in a pattern resembling cobblestones become irregularly shaped and tend to detach from the tumor site in an uncoordinated way — hallmarks
of metastasis.
Some
of the genes involved help regulate the flow
of ions in and
out of the
cells, particularly nerve
cells; others code for so - called heat shock
proteins that are typically induced during stress.
To figure
out the identities
of the host -
cell targets, Linhardt's team, led by graduate student So Young Kim at the Rensselaer Polytechnic Institute, mixed the envelope
protein with sugars called glycosaminoglycans, which the dengue virus uses for this purpose.
This turned
out to be a normal
protein in the
cells of organisms throughout the animal kingdom — but in brains infected with scrapie and related diseases it turns up in both a normal, soluble form and an abnormal, insoluble form which accumulates in deposits that eventually kill the
cells.
«Activation
of these
cell receptors appear to prevent brain
cells from cleaning
out the trash — the toxic buildup
of proteins, such as alpha - synuclein, tau and amyloid, common in neurodegenerative diseases,» says the study's senior author, neurologist Charbel Moussa, MBBS, PhD, director
of Georgetown's Laboratory for Dementia and Parkinsonism, and scientific and clinical research director
of the GUMC Translational Neurotherapeutics Program.
Sommer and his colleagues think that Ubc7p in the
cell's cytoplasm binds to Cue1p, forming a complex that both escorts misfolded
proteins out of the ER and tags them for destruction.
It is those
proteins that carry
out the vital functions
of the
cell.
The conventional view is that the main function
of RNA is to convey instructions from DNA to the
protein - making factories in
cells — a task carried
out by large molecules
of «messenger» RNA.
These
cells turned
out to be very similar to those with Huntington's pathology, corroborating the idea that a lack
of the
protein — not an excess
of it — is driving the disease.
When Gillian Bates at Guy's Hospital, London and Stephen Davies at University College in London and their colleagues examined the brains
of transgenic mice endowed with a DNA encoding 150
of these glutamine repeats, they found that the
protein started
out, at birth, in the cytoplasm
of the animals» brain
cells and then gradually migrated to
cell nuclei and clumped there.
It makes copies
of the virus» genetic material — the viral RNA — to package into new viruses that can infect other
cells; and it reads
out the instructions in that genetic material to make viral messenger RNA, which directs the infected
cell to produce the
proteins the virus needs.
But fortunately our
cells have their own maintenance engineers, in the form
of proteins that cut
out and replace mutated DNA.
In a report published in the Aug. 4 issue
of Science Signaling, Lei Zheng, M.D., Ph.D., and his colleagues show that annexin A2 helps usher a
protein called Sema3D
out of pancreatic cancer
cells.
In what many say is the scientific equivalent
of scaling Mount Everest, researchers have figured
out almost the entire structure
of one part
of the ribosome, the
cell's giant
protein factory.
Tavazoie points
out that «it is remarkable that within a single
cell type, synonymous changes in genetic sequence can dramatically affect the levels
of specific
proteins, their transcripts, and the way a
cell behaves.»
Cells take a number
of complicated steps to translate their sequence
of basic DNA building blocks into
proteins, which then act as workhorses to carry
out the vital functions
of life.
When the researchers used gene engineering techniques to knock
out DDX3 expression in laboratory - grown
cell cultures that highly expressed this
protein,
cell proliferation was half that
of cell cultures with high DDX3 expression.
At any given moment, the human genome spells
out thousands
of genetic words telling our
cells which
proteins to make.
Wondering why the third
protein, an enzyme called p66, was not, despite being very similar to the other two, Pelicci's team knocked
out the piece
of the gene that enabled it to code for p66, in order to make mice and mouse embryonic
cells that lacked p66.
But it does have genes for many types
of transporter
proteins, which ferry molecules into and
out of the
cell.
In order to figure
out which phase that chem7 actually acts upon, Ueda and her team used two fluorescent
proteins of different colors to visualize the process
of the
cell cycles in the root
of Arabidopsis thaliana.
For fruit flies, the fountain
of youth may be filled with an energy - sensing
protein usually activated when
cells are running
out of steam.
The rockets work like this: A
protein anchored to the bacterium's membrane triggers the rapid polymerization
of the
protein actin; this provides an explosive boost, so the bacterium can push through the membrane
of white blood
cells and burst
out to infect another
cell.
Researchers at the Institute
of Science and Technology Austria (IST Austria) now solved a part
of this puzzle by studying how the bacterium Escherichia coli divides up a
protein complex that detoxifies
cells by pumping multiple drugs such as antibiotics
out of the
cell.
We already knew that E. coli can grip to human
cells using hair - like appendages that have tiny
protein hooks on their tips, but until now no one had worked
out the structure
of this
protein, called FimH, or how it interacts with human
cells.